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http://dx.doi.org/10.1016/j.gie.2020.05.034 | DOI Listing |
Zhonghua Wei Chang Wai Ke Za Zhi
November 2024
Department of General Surgery, the Affiliated Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai200127, China.
To explore the long-term prognosis of surgical treatment for peri-gastric cardial gastrointestinal stromal tumors (GISTs). In this retrospective cohort study, we analyzed selected data of patients with peri-gastric cardial GISTs who had undergone radical surgery in Renji Hospital, Shanghai Jiao Tong University School of Medicine, from May 1998 to December 2020. Inclusion criteria comprised radical surgery, pathologically confirmed primary gastric GIST; tumor involving the cardia or within 5 cm of the cardia dentate line; and relatively complete clinical data, including adjuvant therapy and follow-up information.
View Article and Find Full Text PDFCase Rep Gastrointest Med
August 2023
University at Buffalo, State University of New York, Buffalo, USA.
Perigastric and intramural gastric hematomas rarely occur, with most cases associated with trauma, coagulopathy, and peptic ulcer disease. Furthermore, hematomas in the upper gastrointestinal tract are commonly located in the esophagus and duodenum. In this case report, we describe a hematoma masquerading as a gastric tumor on esophagogastroduodenoscopy (EGD) in a 54-year-old male presenting with melena.
View Article and Find Full Text PDFCase Rep Gastroenterol
August 2021
Internal Medicine, BronxCare Health System, Bronx, New York, USA.
Gastrointestinal stromal tumors (GISTs) are the stromal or mesenchymal neoplasms affecting the gastrointestinal tract. Although they constitute 1% of primary gastrointestinal tumors, they are the most common nonepithelial tumors involving the gastrointestinal tract. They mostly present as overt or occult gastrointestinal bleeding.
View Article and Find Full Text PDFMedicine (Baltimore)
October 2020
Division of General Surgery, Department of Surgery, Taipei Veterans General Hospital.
Rationale: Paragangliomas (PGLs) are rare neuroendocrine tumors that are strongly influenced by genetics, and succinate dehydrogenase-deficient PGLs appear to constitute one of the most important categories. Interestingly, somatic PGLs only possess genomic alterations involving the SDHB and SDHD subunits, and no SDHA alterations have been described. Here, we are presenting the clinical and genetic analyses of 2 cases with the first somatic SDHA variant identified in PGLs.
View Article and Find Full Text PDFGastrointest Endosc
November 2020
Division of Gastroenterology and Hepatology, The University of New Mexico School of Medicine, Albuquerque, New Mexico, USA.
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